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Article in English | IMSEAR | ID: sea-94723

ABSTRACT

Papillon Lefèvre syndrome is a rare disease characterized by skin lesions caused by palmar-plantar hyperkeratosis, and severe periodontal destruction involving both the primary and permanent dentitions. It is transmitted as an autosomal recessive condition and consanguinity of parents is evident in about one-third of cases. Pyogenic liver abscess is an increasingly recognized complication. We report a new case of this association and review the current literature.


Subject(s)
Adolescent , Ceftriaxone/administration & dosage , Chromosomes, Human, Pair 11 , Cathepsin C/genetics , Genes, Recessive , Gentamicins/administration & dosage , Humans , Keratoderma, Palmoplantar/genetics , Liver Abscess, Pyogenic/genetics , Male , Mutation , Papillon-Lefevre Disease/drug therapy , Periodontal Diseases/genetics
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